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Prenatal Ad.VEGF Gene Therapy Increases Fetal Growth Velocity and Expression of VEGF Receptors in an Ovine Paradigm of Fetal Growth Restriction. DJ Carr , RP Aitken , JS Milne, DM Peebles, J Martin, I Zachary, JM Wallace, AL David
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Prenatal Ad.VEGF Gene Therapy Increases Fetal Growth Velocity and Expression of VEGF Receptors in an Ovine Paradigm of Fetal Growth Restriction DJ Carr, RP Aitken, JS Milne, DM Peebles, J Martin, I Zachary, JM Wallace, AL David Prenatal Cell and Gene Therapy Group, UCL Institute for Women’s Health Rowett Institute of Nutrition and Health, University of Aberdeen Centre for Cardiovascular Medicine and Biology, UCL
Complicates 8% of pregnancies (severe in 1:500) • Major cause of perinatal mortality and morbidity • No effective treatment • Outcome dependent on gestational age • Reduced uterine blood flow (in early onset FGR) Fetal Growth Restriction – FGR
Prenatal Ad.VEGF Gene Therapy • Uterine artery injection of Ad.VEGF (adenoviral constructs encoding • vascular endothelial growth factor gene) in normal sheep pregnancy • increases uterine blood flow for at least 4 weeks (Mehta et al. 2011) Ad.VEGF 40 % increase Ad.LacZ 16 % increase
58th Annual SGI Meeting, March 2011 • Ad.VEGF treatment of growth-restricted sheep fetuses: • Significant increase in fetal growth velocity • (maximum effect observed 3 to 4 weeks post-treatment) • Tendency towards increased lamb birth weight near to term p=0.081 * * * p=<0.05
↓ Fetal weight (30-40%) ↓ Placental size ↓ Gestation length ↑ Perinatal mortality ↓ Placental vascularity ↓ Placental angiogenic factors ↓ Placental hormone production ↓ Uterine blood flow (42%) (Wallace 1996–2011) Overnourished Adolescent Paradigm of FGR
Aims • To determine the effects of Ad.VEGF therapy in FGR on: • Serial measurements of uterine blood flow • Fetal growth (relative to normally growing controls) • Fetal weight and fetal body composition in late gestation • Placental expression of selected angiogenic factors/receptors
1. Superovulation + laparoscopic intrauterine insemination (single sire) Materials and Methods 2. Embryo Recovery • Singletons • Known gestational age • Maximised genetic homogeneity Embryo Recovery 3. Embryo Transfer
Experimental Design n = 57 Viable pregnancies n = 45 High intake n = 12 Control intake
Uterine artery injection (mid-gestation) Overnourished ewes randomised to Ad.VEGF, Ad.LacZ or Saline
Experimental Design n = 57 Viable pregnancies n = 45 High intake n = 12 Control intake +Saline +LacZ +Saline +Ad.VEGF n = 12 Control n = 18 VEGF n = 13 Saline n = 14 LacZ
Abdominal circumference Biparietal diameter Umbilical artery Dopplersl Renal length Renal transverse / AP diameters Deepest vertical pool of liquor
Fetal Cotyledon Necropsy (D131) and Placental Analyses Uterine Wall Maternal Caruncle • Placentome separated into maternal (caruncular) • and fetal (cotyledonary) portions and snap frozen • RNA extracted and reversed transcribed to cDNA • Quantitative RT-PCR for eNOS, VEGF, Flt1 and KDR
Fetal Growth Velocity A p = 0.031 / p = 0.047 B p = 0.032 / p = 0.016
Proportions of Fetuses >2SD Below Control Mean (Control mean = 5084g , SD = 431g, >2SD cut-off = 4222g) FGR >2SD FGR <2SD p = 0.033 (Fisher’s exact test) Saline+LacZ VEGF
Serial Ultrasound BPD to AC Ratios A p = 0.007 / p = 0.016 B p = 0.016 / p = <0.001 C p = <0.001 / p = <0.001
Indices of Fetal Brain Sparing at Necropsy: Relative Brain Weight (g/kg)Brain:Liver Weight Ratio p=0.046 p=0.009 p=0.001 p=<0.001
Placental mRNA Expression: VEGF & eNOS VEGF / 18s eNOS / 18s
Placental mRNA Expression: Flt1 & KDR Flt1 / 18s KDR / 18s
Ad.VEGF treatment in the overnourished adolescent sheep paradigm of FGR resulted in: • Increased fetal growth velocity relative to untreated FGR groups (maximum effect 3 to 4 weeks post- administration) • Fewer fetuses >2SD below control mean in late gestation • Evidence of an attenuated brain sparing effect: • ↓ BPD:AC ratios on serial ultrasound examination • ↓ relative brain weight / brain to liver weight ratio • No measurable effect on uterine blood flow • Increased caruncular mRNA expression of Flt1 and KDR Summary
Acknowledgements Funded by the Wellcome Trust, Wellbeing of Women and Ark Therapeutics plc